State
73,806 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,054 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 708 (23%) are Severe.
Which agencies issued them
These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Time-Cap Laboratories is recalling specific lots of Ibuprofen Tablets USP 600 mg due to odor complaints linked to CGMP deficiencies.
Crimson Trace is recalling 184,390 laser sights for firearms because some units exceeded the 5 mW power output limit.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur CA 125II Assay kits because some patient samples may exhibit over-recovery outside the provided data.
Howmedica Osteonics Corp. is recalling 77 Triathlon Revision Knee implants because customers may receive the incorrect size from what is labeled on the box.
Diagnostic Hybrids, Inc. is recalling 107 MicroVue SC5b-9 Plus EIA kits because a component was found to contain bacterial contamination.
Time-Cap Laboratories is recalling specific lots of Ibuprofen Tablets USP 400 mg due to odor complaints related to CGMP deficiencies.
McKesson Packaging Services is recalling Diltiazem CD 180 mg capsules because stability testing showed high dissolution results.
Time-Cap Laboratories is recalling specific lots of Ibuprofen Caplets 200 mg due to odor complaints and CGMP deficiencies. The recall covers nationwide distribution.
Zimmer Biomet is recalling Smooth Guide Wire Bullet Tip products because the sterile packaging seal may fail, potentially compromising sterility.
Keystone Dental Inc is recalling 19 Genesis Surgical Cassettes because extra-large grommets cause dental burrs to wobble.
Menarini Silicon Biosystems is recalling CellSearch Circulating Tumor Cell Kits because unusually high image counts may delay result reporting.
CooperVision is recalling specific lots of Clariti 1 Day contact lenses because the secondary packaging displays an incorrect expiration date.
McKesson Packaging Services is recalling Diltiazem HCl Extended-Release Capsules because stability testing showed high dissolution results, failing specifications.
CooperVision is recalling Clariti 1 Day contact lenses because the secondary packaging displays an incorrect expiration date.
CooperVision is recalling Clariti 1 Day contact lenses because the secondary packaging displays an incorrect expiration date.
CooperVision is recalling Clariti 1 Day contact lenses because the secondary packaging displays an incorrect expiration date.
Chrysler is recalling 2018 Jeep Cherokee vehicles with 2.4L engines because a fuel tube may leak, increasing the risk of a fire.
Chrysler is recalling 2018 Jeep Compass vehicles because front lower control arms may be incorrectly welded, potentially causing separation and loss of vehicle control.
Chrysler is recalling 2004-2007 Jeep Liberty vehicles because rear suspension lower control arms can fracture due to corrosion, potentially causing a loss of vehicle control.
Chrysler is recalling specific Mopar Gooseneck Ball Kits because the retention ball may detach from the truck, increasing the risk of a crash.
Chrysler is recalling 2018 RAM 4500 and 5500 trucks because brake hose ferrules may lack anti-corrosion plating, potentially causing fluid leaks and loss of braking.
Chrysler is recalling 2018 Dodge, Jeep, Chrysler, and RAM vehicles because an incorrect transmission park lock rod may prevent the vehicle from staying in Park, increasing crash risk.
Chrysler is recalling 2015-2018 Dodge Charger pursuit police vehicles because the front driveshaft may detach, creating a road hazard and increasing crash risk.
Premier Kitchen Products is recalling Sharper Image and Frigidaire mandoline slicers because small blades can separate, posing a laceration hazard. No injuries have been reported.
Ford is recalling 25,658 2015-2017 Transit vehicles with trailer tow modules because water intrusion can corrode wiring, potentially causing electrical shorts, fires, or crashes.